"Fulgent Genetics, Fulgent Genetics"[submitter] AND "WDR36"[gene] - ClinVar

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	Variation	Gene (Protein Change)	Type (Consequence)	Condition	Classification, Review status
Select item 1581	NM_139281.3(WDR36):c.896A>G (p.Asn299Ser)	WDR36 (N299S)	Single nucleotide variant (missense variant)	Glaucoma 1, open angle, G +1 more	GConflicting classifications of pathogenicity
Select item 1247765	NM_139281.3(WDR36):c.1717-20_1717-19insATATA	WDR36	Insertion (intron variant)	Glaucoma 1, open angle, G +1 more	GBenign/Likely benign
Select item 1229384	NM_139281.3(WDR36):c.1717-20T>A	WDR36	Single nucleotide variant (intron variant)	not provided +1 more	GBenign/Likely benign

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